EP0621253B2 - Process for preparing cyclopentenones - Google Patents
Process for preparing cyclopentenones Download PDFInfo
- Publication number
- EP0621253B2 EP0621253B2 EP94102058A EP94102058A EP0621253B2 EP 0621253 B2 EP0621253 B2 EP 0621253B2 EP 94102058 A EP94102058 A EP 94102058A EP 94102058 A EP94102058 A EP 94102058A EP 0621253 B2 EP0621253 B2 EP 0621253B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- organic solvent
- process according
- mixture
- phase
- product
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/65—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups
- C07C45/66—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by splitting-off hydrogen atoms or functional groups; by hydrogenolysis of functional groups by dehydration
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/597—Unsaturated compounds containing a keto groups being part of a ring of a five-membered ring
Definitions
- This process relates to the preparation of 3-methylcyclopent-2-en-1-one from a 1,4-diketone.
- Cyclopentenones are useful compounds for preparing hydrocarbyl substituted cyclopentadienes which can be reacted with transition metal salts to form metallocene catalysts for olefin polymerization. It is known to make cyclopentenones, such as 3-methylcyclopent-2-en-1-one, by heating a 1,4-diketone, such as acetonylacetone, with base, such as NaOH. The product is unstable in the presence of base. Consequently, either care must be taken to avoid excessive tar formation or the product must be removed as it is formed, for example, by distillation as described in U.S. Patent No. 3,907,896.
- U.S.-P-5,276,199 relates to a process for preparing a cyclopentenone by forming a two-phase mixture of a 1,4-diketone, a water immiscible organic solvent and an aqueous base solution and heating the mixtures so as to convert 1,4-diketone to a cyclopentenone which collects in the organic solvent base.
- a process for preparing 3-methylcyclopent-2-en-1-one comprises forming a two-phase mixture of acetonylacetone, a water immiscible organic solvent and an aqueous base solution, and heating the mixture to a temperature of from 50 to 100°C so as to convert the acetonylacetone to 3-methylcyclopent-2-en-1-one which collects in the organic solvent phase.
- 1,4-diketone reactants for use in the process of the invention can be prepared as known in the art, for example, see Rosini G. et al. Tetrahedron , 39 (24) 4127-32 (1983).
- the reaction mixture is a two-phase system which includes an aqueous phase and an organic solvent phase.
- the aqueous phase comprises an aqueous solution of a base such as an alkali metal hydroxide solution, for example, sodium or potassium hydroxide.
- a base such as an alkali metal hydroxide solution, for example, sodium or potassium hydroxide.
- sodium hydroxide is used in amounts to provide a 0.5 to 5 molar aqueous NaOH solution.
- the organic solvent phase comprises a substantially water immiscible organic solvent, preferably hydrocarbyl or hydrocarbyl halide solvents and mixtures thereof having a boiling point of from 25 to 250°C.
- solvents include aromatic solvents such as toluene, xylenes, benzene, mesitylene, and the like and aliphatic solvents such as cyclohexane, hexanes, heptanes, octanes, methylene chloride, methylene bromide, ethylene dichloride, ethylene dibromide, and the like.
- the lower boiling solvents can be employed in a closed system.
- the proportions of water and organic solvents in the two phase system preferably range from 0.5 to 10 parts by volume water per part by volume of organic solvent.
- the proportion of ketone reactant to base preferably ranges from 0.5 to 5 moles of ketone per mole of base.
- the reaction is carried out with mixing to promote contact between the phases at temperatures of from 50 to 100°C and preferably from 70 to 85°C. Typical reaction times range from 0.5 to 20 hours.
- the cyclopentenone product collects in the organic solvent phase such that product contact with the base is minimized. In this way, product decomposition due to such contact is reduced. Higher base concentrations aid in the "salting out" of the product into the organic phase.
- the product can be recovered from the organic phase by conventional techniques such as by washing the organic layer with water or aqueous, saturated NaCl and then removing the organic solvent such as by vacuum stripping.
- the aqueous base layer can be extracted with an organic solvent to recover any product which remains in the aqueous layer.
- Acetonylacetone (0.20 mol. 22.8g) and toluene (26 ml) were placed in a 100 mL 3-necked, round bottom flask equipped with a thermometer and magnetic stirring bar.
- a mixture of NaOH (2.0 g, 0.05 mol) and water (20.0 g) was added at 22°C into the above flask.
- This two-layer mixture was then stirred and heated at 80-85°C for a period of six hours.
- GC analysis showed a 98% conversion of acetonylacetone.
- the color of the two-phase mixture was dark brown and some tar formation was observed.
- the toluene layer was separated and washed once with 10 ml of saturated NaCl solution.
- the toluene was stripped off at 30-40°C (20 mm Hg) and the product 3-methylcyclopent-2-en-1-one was collected by distillation at 45-70°C (5-15 mm Hg).
- the product weighed 9.96 g and GC analysis showed a 92% purity (48% yield) and 8% toluene.
- the color of product is pale yellow.
- Acetonylacetone (0.10 mol. 11.4g) and CH 2 Br 2 (40 ml) were placed in a 250 mL 3-necked, round bottom flask equipped with a thermometer and magnetic stirring bar.
- a mixture of NaOH (4.0 g, 0.10 mol) and water (96.0 g) was added at 22°C into the flask.
- This two-layer mixture was stirred at 85°C over a period of two hours.
- GC analysis showed a complete conversion of acetonylacetone. The color of this two-phase mixture was dark brown and some tar formation was observed.
- the CH 2 Br 2 layer was separated and the aqueous layer was extracted once with CH 2 Br 2 (10 ml) which was then added to the CH 2 Br 2 layer.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
- This process relates to the preparation of 3-methylcyclopent-2-en-1-one from a 1,4-diketone.
- Cyclopentenones are useful compounds for preparing hydrocarbyl substituted cyclopentadienes which can be reacted with transition metal salts to form metallocene catalysts for olefin polymerization. It is known to make cyclopentenones, such as 3-methylcyclopent-2-en-1-one, by heating a 1,4-diketone, such as acetonylacetone, with base, such as NaOH. The product is unstable in the presence of base. Consequently, either care must be taken to avoid excessive tar formation or the product must be removed as it is formed, for example, by distillation as described in U.S. Patent No. 3,907,896.
- U.S.-P-5,276,199 relates to a process for preparing a cyclopentenone by forming a two-phase mixture of a 1,4-diketone, a water immiscible organic solvent and an aqueous base solution and heating the mixtures so as to convert 1,4-diketone to a cyclopentenone which collects in the organic solvent base.
- We have now discovered an improved process for preparing 3-methylcyclopent-2-en-1-one, which can be carried out at lower temperatures and does not involve the contemporaneous removal of product from the reaction mixture. This invention also provides a practical process in which the reactor-loading can be 5-10 times higher than in the process according to the above mentioned patent.
- In accordance with this invention there is provided a process for preparing 3-methylcyclopent-2-en-1-one, which process comprises forming a two-phase mixture of acetonylacetone, a water immiscible organic solvent and an aqueous base solution, and heating the mixture to a temperature of from 50 to 100°C so as to convert the acetonylacetone to 3-methylcyclopent-2-en-1-one which collects in the organic solvent phase.
- The 1,4-diketone reactants for use in the process of the invention can be prepared as known in the art, for example, see Rosini G. et al. Tetrahedron, 39 (24) 4127-32 (1983).
- The reaction mixture is a two-phase system which includes an aqueous phase and an organic solvent phase.
- The aqueous phase comprises an aqueous solution of a base such as an alkali metal hydroxide solution, for example, sodium or potassium hydroxide. Preferably, sodium hydroxide is used in amounts to provide a 0.5 to 5 molar aqueous NaOH solution.
- The organic solvent phase comprises a substantially water immiscible organic solvent, preferably hydrocarbyl or hydrocarbyl halide solvents and mixtures thereof having a boiling point of from 25 to 250°C. Non-limiting examples of solvents include aromatic solvents such as toluene, xylenes, benzene, mesitylene, and the like and aliphatic solvents such as cyclohexane, hexanes, heptanes, octanes, methylene chloride, methylene bromide, ethylene dichloride, ethylene dibromide, and the like. The lower boiling solvents, can be employed in a closed system.
- The proportions of water and organic solvents in the two phase system preferably range from 0.5 to 10 parts by volume water per part by volume of organic solvent. The proportion of ketone reactant to base preferably ranges from 0.5 to 5 moles of ketone per mole of base.
- The reaction is carried out with mixing to promote contact between the phases at temperatures of from 50 to 100°C and preferably from 70 to 85°C. Typical reaction times range from 0.5 to 20 hours.
- During the reaction, the cyclopentenone product collects in the organic solvent phase such that product contact with the base is minimized. In this way, product decomposition due to such contact is reduced. Higher base concentrations aid in the "salting out" of the product into the organic phase. When the reaction is complete, the product can be recovered from the organic phase by conventional techniques such as by washing the organic layer with water or aqueous, saturated NaCl and then removing the organic solvent such as by vacuum stripping. The aqueous base layer can be extracted with an organic solvent to recover any product which remains in the aqueous layer.
- The invention is further illustrated by, but is not intended to be limited to, the following examples.
- Acetonylacetone (0.20 mol. 22.8g) and toluene (26 ml) were placed in a 100 mL 3-necked, round bottom flask equipped with a thermometer and magnetic stirring bar. A mixture of NaOH (2.0 g, 0.05 mol) and water (20.0 g) was added at 22°C into the above flask. This two-layer mixture was then stirred and heated at 80-85°C for a period of six hours. GC analysis showed a 98% conversion of acetonylacetone. The color of the two-phase mixture was dark brown and some tar formation was observed. The toluene layer was separated and washed once with 10 ml of saturated NaCl solution. The toluene was stripped off at 30-40°C (20 mm Hg) and the product 3-methylcyclopent-2-en-1-one was collected by distillation at 45-70°C (5-15 mm Hg). The product weighed 9.96 g and GC analysis showed a 92% purity (48% yield) and 8% toluene. The color of product is pale yellow.
- Acetonylacetone (0.10 mol. 11.4g) and CH2Br2 (40 ml) were placed in a 250 mL 3-necked, round bottom flask equipped with a thermometer and magnetic stirring bar. A mixture of NaOH (4.0 g, 0.10 mol) and water (96.0 g) was added at 22°C into the flask. This two-layer mixture was stirred at 85°C over a period of two hours. GC analysis showed a complete conversion of acetonylacetone. The color of this two-phase mixture was dark brown and some tar formation was observed. The CH2Br2 layer was separated and the aqueous layer was extracted once with CH2Br2 (10 ml) which was then added to the CH2Br2 layer. The combined CH2Br2 solution was washed once with 10 ml of water and then dried over 4A molecular sieves. The CH2Br2 was stripped off at 30-40°C (20 mm Hg) and the product 3-methyl-cyclopent-2-en-1-one was collected at 70-75° (15 mm Hg). The product weighed 5.44 g (57% yield) and GC analysis showed a 97% purity. The color of product is pale yellow.
Claims (8)
- A process for preparing 3-methylcyclopent-2-en-1-one, which process comprises forming a two-phase mixture of acetonylacetone, a water immiscible organic solvent, and an aqueous base solution, and heating said mixture to a temperature of from 50 to 100 °C so as to convert the acetonylacetone to 3-methylcyclopent-2-en-1-one which collects in the organic solvent phase.
- The process according to claim 1 wherein said aqueous base solution is an aqueous sodium hydroxide solution.
- The process according to claim 2 wherein said aqueous base solution is a 0.5 to 5 molar aqueous sodium hydroxide solution.
- The process according to any of the preceding claims wherein said organic solvent is a hydrocarbyl or hydrocarbyl halide solvent.
- The process according to any of the preceding claims wherein the proportions of water and organic solvent range from 0.5 to 10 parts by volume of water per part by volume of organic solvent.
- The process according to any of the preceding claims wherein said mixture is heated to a temperature in the range of from 70 to 85°C.
- The process according to any of the preceding claims wherein said organic solvent is toluene or methylene dibromide.
- The process according to claim 7 wherein said mixture is heated to a temperature in the range of from 80 to 85°C.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/016,447 US5276199A (en) | 1993-02-11 | 1993-02-11 | Process for preparing cyclopentenones |
US16447 | 1993-02-11 |
Publications (4)
Publication Number | Publication Date |
---|---|
EP0621253A2 EP0621253A2 (en) | 1994-10-26 |
EP0621253A3 EP0621253A3 (en) | 1995-02-01 |
EP0621253B1 EP0621253B1 (en) | 1997-07-30 |
EP0621253B2 true EP0621253B2 (en) | 2000-08-09 |
Family
ID=21777168
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94102058A Expired - Lifetime EP0621253B2 (en) | 1993-02-11 | 1994-02-10 | Process for preparing cyclopentenones |
Country Status (5)
Country | Link |
---|---|
US (1) | US5276199A (en) |
EP (1) | EP0621253B2 (en) |
JP (1) | JP3553118B2 (en) |
CA (1) | CA2113322C (en) |
DE (1) | DE69404529T3 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5276199A (en) * | 1993-02-11 | 1994-01-04 | Ethyl Corporation | Process for preparing cyclopentenones |
US5939347A (en) * | 1995-01-25 | 1999-08-17 | W.R. Grace & Co. -Conn. | Supported catalytic activator |
US5763664A (en) * | 1995-12-01 | 1998-06-09 | Albemarle Corporation | Process for preparing cyclopentenones |
WO1998040341A1 (en) * | 1997-03-10 | 1998-09-17 | Hanil Synthetic Fiber Co., Ltd. | Process for preparation of cyclopentenones in supercritical fluids |
KR100614395B1 (en) * | 2004-05-24 | 2006-08-18 | 주식회사 엘지화학 | Process For Preparing Cyclopentenones |
CN105294418B (en) * | 2015-11-11 | 2017-07-25 | 中国科学院山西煤炭化学研究所 | A kind of method for preparing the ketone of 3 methyl, 2 cyclopentene 1 |
CN112028757B (en) * | 2020-09-08 | 2022-04-05 | 乐威医药(江苏)股份有限公司 | Preparation method of 3-methyl-2-cyclopentene-1-ketone |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2387587A (en) † | 1939-01-04 | 1945-10-23 | Hunsdiecker Heinz | Process of manufacturing cyclopentenone derivatives |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE765015C (en) * | 1939-01-05 | 1952-09-29 | Heinz Hunsdiecker Dr | Process for the Preparation of Aliphatically Substituted Cyclopentenones by Cyclization of ª-Diketones (2,5-Diketones) |
CH566953A5 (en) * | 1972-04-07 | 1975-09-30 | Givaudan & Cie Sa | |
JPS52122344A (en) * | 1976-04-05 | 1977-10-14 | Tatsuya Shiyouno | Process for manufacture of cyclopentenone derivatives |
IT1170704B (en) * | 1981-02-11 | 1987-06-03 | Giovanni Piancatelli | PROCEDURE FOR THE SYNTHESIS OF 3-KETOCYCLOPENTENE-5-BONE DERIVATIVES WITH INSECTICIDE ACTIVITY |
US5026919A (en) * | 1985-12-20 | 1991-06-25 | Mobil Oil Corporation | Base-catalyzed reactions using zeolite catalysts |
US5276199A (en) * | 1993-02-11 | 1994-01-04 | Ethyl Corporation | Process for preparing cyclopentenones |
-
1993
- 1993-02-11 US US08/016,447 patent/US5276199A/en not_active Expired - Lifetime
-
1994
- 1994-01-12 CA CA002113322A patent/CA2113322C/en not_active Expired - Lifetime
- 1994-02-08 JP JP03429494A patent/JP3553118B2/en not_active Expired - Lifetime
- 1994-02-10 DE DE69404529T patent/DE69404529T3/en not_active Expired - Lifetime
- 1994-02-10 EP EP94102058A patent/EP0621253B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2387587A (en) † | 1939-01-04 | 1945-10-23 | Hunsdiecker Heinz | Process of manufacturing cyclopentenone derivatives |
Non-Patent Citations (7)
Title |
---|
Advanced Org. Chem., 3rd ed., 1985, pp. 829-831 † |
Blaise, Compt. Rend., 1914, vol. 158, p. 708 † |
Handbook of Chem. and Phys., 66th ed., 1985, p. D-12 † |
Helv. Chim. Acta, 1978, vol. 61, pp. 990-997 † |
J. Chem. Soc., 1950, pp. 3634-3641 † |
J. Chem. Soc., 1952, pp. 1127-1133 † |
Org. Reactions, 1968, vol. 16, pp. 1-77, J. Wiley † |
Also Published As
Publication number | Publication date |
---|---|
DE69404529T2 (en) | 1997-12-04 |
DE69404529D1 (en) | 1997-09-04 |
EP0621253B1 (en) | 1997-07-30 |
JPH06340571A (en) | 1994-12-13 |
CA2113322C (en) | 2005-07-26 |
DE69404529T3 (en) | 2001-02-01 |
CA2113322A1 (en) | 1994-08-12 |
US5276199A (en) | 1994-01-04 |
JP3553118B2 (en) | 2004-08-11 |
EP0621253A3 (en) | 1995-02-01 |
EP0621253A2 (en) | 1994-10-26 |
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